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自发性脊柱骨膜外动静脉瘘合并长节段显著硬膜外静脉引流致严重压迫性胸段脊髓病,经血管内和手术联合治疗成功:病例报告及文献复习

Spontaneous Spinal Osseous Epidural Arteriovenous Fistula with Long Segments of Prominent Epidural Venous Drainage Causing Severe Compressive Thoracic Myelopathy Successfully Treated with Combined Endovascular and Surgical Treatments: A Case Report and Review of the Literature.

作者信息

Iampreechakul Prasert, Tirakotai Wuttipong, Lertbutsayanukul Punjama, Thammachantha Samasuk, Siriwimonmas Somkiet

机构信息

Department of Neurosurgery, Prasat Neurological Institute, Bangkok, Thailand.

Department of Neuroradiology, Prasat Neurological Institute, Bangkok, Thailand.

出版信息

Asian J Neurosurg. 2020 Oct 19;15(4):1041-1049. doi: 10.4103/ajns.AJNS_353_20. eCollection 2020 Oct-Dec.

Abstract

The authors describe an extremely rare case of spinal osseous epidural arteriovenous fistulas (SOEAVFs) with unique characteristic features. A 25-year-old man presented with progressive weakness and paresthesia of the lower extremities for 1 month. Magnetic resonance imaging of the thoracic spine showed an extradural dilated vascular flow void structure extending from T4 to T8 levels with abnormal hyperintense T2 signal from T6 to T8 levels. Magnetic resonance angiography and spinal angiography revealed unique features of SOEAVF supplied by multiple small arterial feeders of intercostal arteries converging into a dilated round venous sac corresponding to a bony defect of T7 lamina and spinous process. The venous drainage directly drained into prominent epidural venous plexus extending from the level of T4 to T8 without intradural venous drainage, causing severe compressive myelopathy. Transarterial embolization was performed using N-butyl cyanoacrylate through the main feeder. Subsequently, he successfully underwent laminectomy and total excision of the fistula and large epidural draining venous plexus. Histopathology confirmed spinal vascular malformations with evidence of previous embolization. He gradually improved until being ability to walk independently 3 months later. Follow-up spinal angiography confirmed complete resection of SOEAVF. The patient has remained clinically asymptomatic 5 years after operation.

摘要

作者描述了一例极为罕见的具有独特特征的脊柱骨膜外动静脉瘘(SOEAVF)。一名25岁男性出现下肢进行性无力和感觉异常1个月。胸椎磁共振成像显示硬膜外扩张的血管流空结构从T4延伸至T8水平,T6至T8水平T2信号异常高。磁共振血管造影和脊髓血管造影显示SOEAVF的独特特征,由多条肋间动脉的小动脉分支供血,汇聚成一个扩张的圆形静脉囊,对应于T7椎板和棘突的骨缺损。静脉引流直接流入从T4至T8水平延伸的突出硬膜外静脉丛,无硬膜内静脉引流,导致严重的压迫性脊髓病。通过主要供血动脉使用氰基丙烯酸正丁酯进行经动脉栓塞。随后,他成功接受了椎板切除术以及瘘管和大型硬膜外引流静脉丛的完全切除。组织病理学证实为脊柱血管畸形,有先前栓塞的证据。他逐渐好转,3个月后能够独立行走。随访脊髓血管造影证实SOEAVF已完全切除。患者术后5年一直无临床症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f343/7869281/48ea1b14eeea/AJNS-15-1041-g001.jpg

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